Taiwan FDA registration 66959ba5e127109bf0a9a951a3647b0e

"Kellos Martin" electrosurgical system

TW: “凱樂思馬丁”電刀系統
Taiwan flagTaiwan·Risk Class 2·KLS MARTIN SE & CO. KG;; KLS Martin SE & Co. KG·Registered May 19, 2020 – May 19, 2030Active
Registration details
Analysis ID
66959ba5e127109bf0a9a951a3647b0e
Customs Code
DHA05603365002
Company information
Manufacturer Country
Germany
Authorized Representative
KLS MARTIN TAIWAN LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4400 Cutting and hemostasis electric knives and accessories thereof
Import Information
import
Dates and status
Registration Date
May 19, 2020
Expiry Date
May 19, 2030
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About this record

Access comprehensive regulatory information for "Kellos Martin" electrosurgical system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 66959ba5e127109bf0a9a951a3647b0e and manufactured by KLS MARTIN SE & CO. KG;; KLS Martin SE & Co. KG. The authorized representative in Taiwan is KLS MARTIN TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including KLS MARTIN SE & CO. KG;; KLS Martin SE & Co. KG, and 2 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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